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Clinical Research Coordinator

LMC’s clinical network is comprised of 11 Healthcare Centres of Excellence, in 3 provinces (Quebec, Ontario and Alberta ).

LMC is proud to have earned 2014 and 2015's Great Places to Work in Canada award.

Currently, our rapidly expanding team is looking for a regional Clinical Research Coordinator who can work for us on a full-time permanent basis, supporting our LMC Calgary site.

Responsibilities will include but are not limited to:

  • To conduct the clinical research study according to the study protocol, GCP, and the LMC Research SOP
  • To be knowledgeable of the protocol so that all study activities are completed correctly
  • To recruit and screen patients for participation in clinical research studies
  • To obtain proper written informed consent from each study participant prior to participation in the study
  • To schedule study participant visits as per protocol
  • To perform delegated protocol specific activities completely and accurately
  • To obtain vital signs as required per protocol (i.e. blood pressure, temperature, heart rate, waist measurement, weight & height)
  • To obtain all necessary documentation as required by the protocol (i.e. ECG, echocardiogram or pulmonary function test results)
  • To monitor and report all adverse experiences and abnormal results to the Investigator and Sponsor
  • To update and maintain subject screening and enrollment logs
  • To create source documents and any other research documents required for the successful conduct of a clinical research study
  • To meet with the Sponsor's representatives to discuss the conduct of the study and review study data
  • Collect and process specimen (blood, urine, etc.) according to the protocol and laboratory manual and procedures.
  • Process other in-house testing i.e. urine sampling, pregnancy tests, ACTH stimulation test, AIC and to maintain accurate source documents
  • Maintenance and shipment of specimens to the appropriate laboratory as indicated in LMC Lab SOP and/or study protocol.
  • Perform Health Inspector duties as required by LMC Health and Safety guidelines

Requirements:

  • University degree / post-grad diploma in a related field, science background required (Certificate, DEC or B.Sc.) or completion of a Laboratory Technician or Assistant program at a recognized College or University
  • Phase I –IV clinical research is considered a strong asset.
  • Strong knowledge of medical terminology
  • Knowledge of general research procedures and regulatory requirements
  • Strong communication and interpersonal skills
  • Detail oriented with exceptional organizational skills
  • Proficiency with MS Office including creating spreadsheets, reports and presentation
  • Phlebotomy experience an asset

LMC seeks dynamic individuals who embrace learning and innovation opportunities and those who contribute to great visioning.

LMC provides four industry-leading programs:

  • Specialist healthcare (publicly-funded) - representing the largest non-academic group of Endocrinologists globally
  • Nationally-accredited Diabetes Education Program
  • Canada's largest Clinical Research network specializing in  Diabetes innovations
  • A network of diabetes focused pharmacies

Why LMC might be right for you!

  • 2016 Certified Best Workplace™
  • 2014 and 2015 Canada’s Best Workplaces™
  • Fantastic culture based on learning and growth
  • Competitive community based salary
  • Comprehensive Health Benefits & Pension matching
  • Financial support and time off for career training and development·
  • Christmas to New Year’s off; Summer Long Weekends
  • State of the art Electronic Medical Records (EMR) environment

LMC is committed to meet the accessibility needs of persons with disabilities in a timely manner. These accommodations will be available upon request. 

We thank all candidates, however, only those candidates selected for an interview will be contacted.

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